Phase 2 Bladder Cancer Trial, Recruiting NCT06257017 Sponsor: Yung NA Condition: Bladder Cancer
Back to Bladder Cancer

Phase 2 Bladder Cancer Trial, Recruiting

NCT06257017
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged between 18 and 70 years old
  • People who are generally well enough to carry out daily activities with little or no limitation (as measured by a standard medical scale called ECOG, with a score of 0 or 1)
  • People who have had, or are scheduled to have, surgery to remove the bladder (with lymph node removal) or surgery to remove the kidney and ureter
  • People whose surgical tissue sample has confirmed a specific type of bladder or urinary tract cancer called transitional cell (urothelial) carcinoma
  • People whose cancer has been staged at a specific level (pT2–4a, N0–2, M0), meaning the cancer has grown into or through the bladder muscle but has not spread to distant parts of the body (confirm with trial site for exact staging details)
  • People whose surgeon was able to remove all visible cancer with no cancer cells left at the edges of the removed tissue, confirmed by a CT or MRI scan of the chest, abdomen, and pelvis within 4 weeks before joining the trial
  • People whose blood and organ function results fall within acceptable ranges in blood tests taken within 28 days before starting treatment — including healthy enough levels of white blood cells, red blood cells, platelets, liver enzymes, and kidney function (confirm with trial site for specific values)
  • People who are able to understand the trial information and provide written consent to participate

Who may not be able to join:

  • People who have received any approved cancer treatment within 3 weeks before enrolling in the trial
  • People who have taken part in another clinical trial involving a treatment within 28 days before enrolling
  • People who have had a different type of cancer (other than this urinary tract cancer) within the past 5 years
  • People who have health conditions that make chemotherapy unsafe, such as reduced kidney function, hearing problems, or poor bone marrow function
  • People who have had a severe allergic reaction or have a known reason they cannot take the chemotherapy drugs cisplatin or gemcitabine
  • People with active or uncontrolled infections, including HIV, hepatitis B, hepatitis C, or tuberculosis
  • People who are pregnant or breastfeeding

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Yung Na, PHD, The University of Hong Kong

Phone: 22554852

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Yung NA
Registry
ClinicalTrials.gov
Start date
2 February 2024
Est. completion
30 September 2025

Where this trial is recruiting

Hong Kong

Primary endpoints

the radiational disease-free survival (rDFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov